Gene entry
VPS13C
vacuolar protein sorting 13 homolog C
- Chromosome
- 15
- Cytoband
- 15q22.2
- Variants (rsID)
- 37
VPS13C is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q22.2). Its official name is “vacuolar protein sorting 13 homolog C”. The reference table lists 37 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs369100678Pathogenicsingle nucleotide variantAutosomal recessive early-onset Parkinson disease 23|Parkinson disease
- rs869312809Pathogenicsingle nucleotide variantAutosomal recessive early-onset Parkinson disease 23|Parkinson disease
- rs869312810Pathogenicsingle nucleotide variantAutosomal recessive early-onset Parkinson disease 23|Parkinson disease
- rs869312811PathogenicDeletionAutosomal recessive early-onset Parkinson disease 23|Parkinson disease
Other listed variants
- rs1981916
- rs2303405
- rs3743295
- rs3784635
- rs4143844
- rs8042267
- rs9920015
- rs12595158
- rs12907567
- rs17271207
- rs17271256
- rs17271305
- rs28440175
- rs28850690
- rs34445138
- rs72747870
- rs72749739
- rs72749746
- rs72749762
- rs73416547
- rs75341202
- rs76797231
- rs78822825
- rs79456076
- rs111631263
- rs112236709
- rs112732813
- rs117240368
- rs118100937
- rs147486877
- rs149663645
- rs190649048
- rs191777860
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.